Helicotylenchus dihystera

Zeng, Yongsan, Ye, Weimin, Tredway, Lane, Martin, Samuel & Martin, Matt, 2012, Taxonomy and morphology of plant-parasitic nematodes associated with turfgrasses in North and South Carolina, USA, Zootaxa 3452, pp. 1-46 : 9

publication ID

https://doi.org/10.5281/zenodo.210165

DOI

https://doi.org/10.5281/zenodo.6171820

persistent identifier

https://treatment.plazi.org/id/B47487DD-8018-816A-F9F1-F897FF4B1910

treatment provided by

Plazi (2016-04-13 03:04:25, last updated 2024-11-26 04:29:47)

scientific name

Helicotylenchus dihystera
status

 

Helicotylenchus dihystera

( Fig. 2 View FIGURE 2 I, J)

Measurements. See Table 3 View TABLE 3 .

Remarks. Helicotylenchus dihystera was described from soil around sugarcane roots ( Saccharum officinarum ) in Harwood, Australia. It is a cosmopolitan species with a wide geographical distribution, occurring in 17 countries in Europe, 28 in Asia, 30 in Africa, three in North America, 18 in Central America and Caribbean, eight in South America, and eight in Oceania (CABI 2010). In the USA, it occurs in Alabama, Arkansas, California, Colorado, Florida, Georgia, Hawaii, Louisiana, Maryland, Mississippi, Missouri, NC, South Dakota and Texas (CABI 2010). This species has a wide host range including sugarcane, potato, banana, rice, tea, avocado, coffee, maize, beans, wheat, rye, oat, sorghum, and turfgrass ( Kinloch 1971; Siddiqi 1972; Lucas et al. 1974). There was a significant correlation between numbers of H. dihystera and reduced growth of Kentucky bluegrass in a landscape setting in Lincoln, Nebraska ( Sumner 1967) and of turf in bowling greens in Adelaide, Australia ( Wallace 1971). In this study, H. dihystera was found in 34 counties in both NC and SC. It had high prevalence in all three management zones (green, fairway and tee) and two grass species (bentgrass and zoysiagrass). Both morphology and morphometrics fit the description of other populations ( Sher 1966; Siddiqi 1972).

Kinloch, R. A. (1971) Florida field crops as hosts of Helicotylenchus dihystera. Nematropica, 1, 38 - 39.

Lucas, L. T., Blake, C. T. & Barker, K. R. (1974) Nematodes associated with bentgrass and bermudagrass golf greens in North Carolina. Plant Disease Reporter, 58, 822 - 824.

Sher, S. A. (1966) Revision of the Hoplolaiminae (Nematoda). VI. Helicotylenchus Steiner, 1945. Nematologica, 12, 1 - 56.

Sumner, D. R. (1967) Nematodes in bluegrass. Plant Disease Reporter, 51, 457 - 460.

Wallace, H. R. (1971) The influence of the density of nematode populations on plants. Nematologica, 17, 154 - 166.

Gallery Image

FIGURE 2. Micrographs of Hoplolaimus galeatus, Scutellonema brachyurum and Helicotylenchus dihystera from turfgrasses in NC and SC. All scale bars = 20 μm. A. Pharyngeal region of H. galeatus. B. Vulval region of H. galeatus. C. Female tail of H. galeatus. D, E. Male tails of H. galeatus. F. Pharyngeal region of S. brachyurum. G. Vulval region of S. brachyurum. H. Female tail of S. brachyurum. I. Pharyngeal region of H. dihystera. J. Vulva and tail region of H. dihystera.

Kingdom

Animalia

Phylum

Nematoda

Class

Secernentea

Order

Tylenchida

SubOrder

Diphtherophorina

Family

Hoplolaimidae

Genus

Helicotylenchus